(2,4-Bis-benzyloxy-5-isopropenyl-phenyl)-[5-(4-methyl-piperazin-1-yl)-1,3-dihydro-isoindol-2-yl]-methanone → HCID 69481061, compound
Reaction equation
C(O[C:9]1[CH:14]=[C:13](OCC2C=CC=CC=2)[C:12]([C:23]([CH3:25])=[CH2:24])=[CH:11][C:10]=1[C:26]([N:28]1[CH2:36][C:35]2[C:30](=[CH:31][CH:32]=[C:33]([N:37]3[CH2:42][CH2:41][N:40]([CH3:43])[CH2:39][CH2:38]3)[CH:34]=2)[CH2:29]1)=[O:27])C1C=CC=CC=1>CO.[Pd]>[CH:23]([C:12]1[CH2:13][CH2:14][CH2:9][CH:10]([C:26]([N:28]2[CH2:36][C:35]3[C:30](=[CH:31][CH:32]=[C:33]([N:37]4[CH2:42][CH2:41][N:40]([CH3:43])[CH2:39][CH2:38]4)[CH:34]=3)[CH2:29]2)=[O:27])[CH:11]=1)([CH3:25])[CH3:24]Participants
Procedure
A mixture of (2,4-bis-benzyloxy-5-isopropenyl-phenyl)-[5-(4-methyl-piperazin-1-yl)-1,3-dihydro-isoindol-2-yl]-methanone (8.61 g, 15.0 mmol) and 10% Pd/C (1.0 g) in methanol (200 mL) was stirred vigorously under a hydrogen atmosphere (˜1 atm) for 18 h at ambient temperature. The mixture was filtered through a plug of Celite and reduced in vacuo to give a purple oil. This residue was purified by column chromatography using an eluant of DMAW120 to give the title compound as its acetate salt. This salt was taken up in MeOH (30 mL) and to the solution was added saturated HCl in EtOAc (20 mL). This mixture was stirred at ambient for 2 h and the solid formed collected by filtration and dried in vacuo to give the title compound as its hydrochloride salt (2.64 g) as a white solid.
Workup
- filtrationThe mixture was filtered through a plug of Celite
- customto give a purple oil
- customThis residue was purified by column chromatography
Sources & evidence
- ORD record
- ord-85fbbc20a5c34a6fb2eb2c6125d4f9c1
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08816087B2
Reaction notes
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